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NCT00127530 · ClinicalTrials.gov registry record · Phase 3

Study of Oral Fampridine-SR in Multiple Sclerosis

A Phase 3 study, sponsored by Acorda Therapeutics.

Completed
Registry status
Phase 3
Development phase
300
Enrollment target

NCT00127530: Completed Phase 3 study, sponsored by Acorda Therapeutics.

NCT00127530 is a Phase 3 study that has completed, run by Acorda Therapeutics. The registered enrollment target is 300 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00127530, a Phase 3 study, has completed, sponsored by Acorda Therapeutics.

COMPLETED
Registry status
Phase 3
Development phase
300 participants
Enrollment target

Study Summary

To assess the safety and efficacy of 10 milligram (mg) twice a day (b.i.d.) Fampridine-SR in patients diagnosed with multiple sclerosis (MS), in a double-blind, placebo-controlled, parallel group study.

Primary Outcome

Patients who showed a faster walking speed for at least three of the four on-drug visits during the double-blind treatment period as compared to the maximum speed for any of the five off-drug visits.

Interventions

  • DRUG Placebo
  • DRUG Fampridine-SR

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2005-05
Est. Completion 2006-09
Phase Phase 3
Acorda Therapeutics

36 total trials

What the finished NCT00127530 record still lists

NCT00127530 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00127530 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00127530 about?

NCT00127530 is a clinical study titled "Study of Oral Fampridine-SR in Multiple Sclerosis". To assess the safety and efficacy of 10 milligram (mg) twice a day (b.i.d.) Fampridine-SR in patients diagnosed with multiple sclerosis (MS), in a double-blind, placebo-controlled, parallel group study.

What is the current status of trial NCT00127530?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 300 participants. The study started on 2005-05. Estimated completion is 2006-09.

What interventions are being tested in trial NCT00127530?

The interventions under investigation include: Placebo (DRUG), Fampridine-SR (DRUG).

Who is sponsoring clinical trial NCT00127530?

This trial is sponsored by Acorda Therapeutics, which has 36 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00127530's enrollment target sits among peer trials

300 1122nd of 2000 higher than 840 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00127530, the US trial registry maintained by the National Library of Medicine. NCT00127530 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.